FDA Medical Device Recalls (openFDA)
Centurion Medical Products: Dialysis Tray, SP560, Sterile, Micropore Surgical Tape, Single Use Rolls, Tri-State Hospital Supply Company Manufacturers of Centurion Healthcare Products Howell, MI
- Recall number
- Z-1938-2010
- Recalling firm
- Centurion Medical Products
- Product
- Dialysis Tray, SP560, Sterile, Micropore Surgical Tape, Single Use Rolls, Tri-State Hospital Supply Company Manufacturers of Centurion Healthcare Products Howell, MI
- Status
- Terminated
- Initiated
- 2010-03-16
- Posted
- 2010-06-30
- Terminated
- 2011-02-09
- Reason
- The 3M micropore tape is under recall due to the tape not performing and needles becoming loose and dislodged.
- Root cause
- Other
- Action
- The firm sent Urgent Recall Product Notices to its two customers dated 3/16/2010. The letter explained that the tape may not adhere properly. The consignees were instructed to remove any kits containing the recalled tape from their inventory, if the tape was used to secure dialysis needles or pressure dressings. If the tape was used for other purposes, the kits could still be used. The recall letter included a reply form for customers to complete and email or fax back. Upon receipt of the form, a Centurion Representative will contact them to retrieve affected product. Customers should contact Matthew Price at 517-546-5400 ext. 1135, if further info is needed.
- Quantity
- 144 kits
- Distribution
- Nationwide Distribution -- AR and OH.
- Lot, serial or model codes
- 912317, 902048, 2008112490, 2009020290, 2009062290 and 2009070690.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FKG
- Firm FEI
- 1824619
- Firm city
- Howell
- Firm state
- MI
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
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Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28